Name | thiosemicarbazide |
Synonyms | TSC ai3-16319 Aminothiourea aminothio-urea N-Aminothiourea 1-Aminothiourea n-aminothiourea 1-amino-2-thioure thiosemicarbazide AKOS BBS-00004328 1-Amino-2-Thiourea 3-thio-semicarbazid 2-Thiosemicarbazide 3-thiosemicarbazide 1-(aminosulfanyl)urea LABOTEST-BB LT01593682 THIOCARBAMOYL HYDRAZIDE HYDRAZINECARBOTHIOAMIDE Calcineurin B homologous protein 3 |
CAS | 79-19-6 |
EINECS | 201-184-7 |
InChI | InChI=1/CH5N3OS/c2-1(5)4-6-3/h3H2,(H3,2,4,5) |
InChIKey | BRWIZMBXBAOCCF-UHFFFAOYSA-N |
Molecular Formula | CH5N3S |
Molar Mass | 91.14 |
Density | 1.221 (estimate) |
Melting Point | 180-183°C (dec.)(lit.) |
Boling Point | 208.6±23.0 °C(Predicted) |
Water Solubility | soluble |
Solubility | Soluble in water (10 mg/ml at 20 °C), ethanol, alcohols, and hot methanol. |
Vapor Presure | 1.15Pa at 25℃ |
Appearance | White crystal |
Color | White to light yellow |
Merck | 14,9361 |
BRN | 506320 |
pKa | pK1:1.5(+1) (25°C,μ=0.1) |
PH | 5-7 (50g/l, H2O, 20℃) |
Storage Condition | Store at +15°C to +25°C. |
Stability | Stable. Incompatible with strong oxidizing agents. |
Sensitive | Sensitive to air and light |
Refractive Index | 1.5800 (estimate) |
MDL | MFCD00007620 |
Physical and Chemical Properties | Appearance: white crystalline melting point: 180-182 ℃ 3-thiosemarbazide; Hydrazinecarbothioamide; TSC3-Thiosemicarbazide; Hydrazinecarbothiamide; TSC |
Use | Thiosemicarbazide, also known as thiosemicarbazone, is an intermediate for the preparation of carbamate insecticide zosaparib and thiadiazole fungicides and rodenticides, and can also be used in the synthesis of anti-tuberculosis drugs such as amidothiuramide and sulfa drugs, rubber additives and synthetic resin additives, it can also be used as an analytical reagent for the quantification of chromium and the identification of aldehydes and ketones; Hexamethylene glycol intermediate. |
Hazard Symbols | T+ - Very toxic |
Risk Codes | R28 - Very Toxic if swallowed R52/53 - Harmful to aquatic organisms, may cause long-term adverse effects in the aquatic environment. R26/27/28 - Very toxic by inhalation, in contact with skin and if swallowed. |
Safety Description | S22 - Do not breathe dust. S26 - In case of contact with eyes, rinse immediately with plenty of water and seek medical advice. S36/37 - Wear suitable protective clothing and gloves. S45 - In case of accident or if you feel unwell, seek medical advice immediately (show the label whenever possible.) S61 - Avoid release to the environment. Refer to special instructions / safety data sheets. S28A - S36/37/39 - Wear suitable protective clothing, gloves and eye/face protection. |
UN IDs | UN 2811 6.1/PG 2 |
WGK Germany | 3 |
RTECS | VT4200000 |
FLUKA BRAND F CODES | 8-9-23 |
TSCA | Yes |
HS Code | 29335995 |
Hazard Class | 6.1 |
Packing Group | II |
Toxicity | LD50 orally in adult Norway rats: 13 mg/kg, Dieke, Proc. Soc. Exp. Biol. Med. 70, 688 (1949) |
White crystalline or white crystalline powder. Melting point 180~181 °c (decomposition). Soluble in water and ethanol, needle-like crystals from water. It is easy to react with aldehydes and ketones to form specific crystal products; It is also easy to react with carboxylic acids.
obtained by heating reaction of thiourea and hydrazine hydrate as raw materials. In addition, with hydrazine hydrate and ammonium thiocyanate as raw materials, using acetaldehyde as catalyst can also be prepared thiosemicarbazide.
This product is an intermediate for organic synthesis, used in the synthesis of anti-tuberculosis drugs amidothiourea and sulfonamide drugs, as well as rodenticide. It can also be used as an analytical reagent for the quantification of chromium and the identification of aldehydes and ketones. In addition, this product is also used as pesticide intermediates, rubber additives and synthetic resin additives.
thiosemicarbazide is toxic, and thiosemicarbazide-containing preparations are toxic. The oral LD50 is 10-15mg/kg for mice and 19mg/kg for rats. Production equipment should be closed, the operator should wear protective equipment. This product is packed in corrugated boxes lined with polyethylene bags. lOkg per case.
storage and transportation according to toxic chemicalsLogP | -1.67 |
NIST chemical information | information provided by: webbook.nist.gov (external link) |
EPA chemical substance information | information provided by: ofmpeb.epa.gov (external link) |
Use | used in the synthesis of anti-tuberculosis drugs amidothiourea and sulfa drugs, used as pesticide intermediates, rubber additives, thiosemicarbazide, also known as thiosemicarbazil, is an intermediate for the preparation of the carbamate insecticide oxaparb, thiadiazole bactericide and rodenticide, it can also be used for the synthesis of anti-tuberculosis drugs, such as aminothiourea and sulfanilamide, rubber additives and synthetic resin additives. It can also be used as an analytical reagent for the quantification of chromium and the identification of aldehydes and ketones. thiosemicarbazide is an important intermediate in organic synthesis, which is commonly used in the synthesis of 2-substituted hydrazin-4-substituted thiazole antibiotics, such as Nifurthiazole. As well as an antiviral drug, e.g., phthalocyanine, etc. used as an analytical reagent for quantitative determination of chromium and identification of aldehydes and ketones; Used as a complexing agent for copper A complexing agent for copper. A precipitant for the determination of chromium. Reagents for the detection of certain metals and sugars, aldehydes, and ketones. Preparation of rodenticides. This product is an intermediate for organic synthesis, used in the synthesis of anti-tuberculosis drugs, ammonia thiourea and sulfa drugs, as well as rodenticides. It can also be used as an analytical reagent for the quantification of chromium and the identification of aldehydes and ketones. In addition, this product is also used as pesticide intermediates, rubber additives and synthetic resin additives. used as analytical reagent |
production method | thiosemicarbazide is prepared by using hydrazine hydrate and ammonium thiocyanate as raw materials and acetaldehyde as catalyst. See the reaction equation: 2H2NNH2 · H2O + H2SO4 →(H2NNH2)2 · H2SO4 +2H2O(H2NNH2)2 · H2SO4 + 2NH4SCN → 2H2NNH2 · HSCN +(NH4)2SO4 first put a certain amount of hydrazine hydrate into three bottles, cool with water, slowly add a certain concentration of sulfuric acid under stirring, keep the temperature below 40 ℃, controlling pH = 4~5 is the end point to get hydrazine sulfate. Then add ammonium thiocyanate, stirring, at 30 ° C to add a certain amount of acetaldehyde (or acetone), and then move the reaction to the Beaker while hot, at room temperature for 4H, precipitation of crystals, after filtration, the product was washed with water and dried, and the yield was more than 80%. In addition, thiourea and hydrazine hydrate may be used as raw materials for heating reaction. 1. Thiourea and hydrazine hydrate were used as raw materials for heating reaction. 2. Hydrazine sulfate is prepared from hydrazine hydrate and sulfuric acid, which reacts with ammonium thiocyanate to produce hydrazine thiocyanate, and then reacts with acetaldehyde to obtain thiosemicarbazide by hydrolysis. |
category | pesticide |
toxicity grade | highly toxic |
Acute toxicity | oral-rat LD50: 9.16 mg/kg |
flammability hazard characteristics | toxic sulfur oxide and nitrogen oxide gases from combustion |
storage and transportation characteristics | The warehouse is ventilated and dried at low temperature; It is stored and transported separately from food raw materials |
extinguishing agent | dry powder, foam, sand |
toxic substance data | information provided by: pubchem.ncbi.nlm.nih.gov (external link) |